Neurofibromin 1 anticorps (AA 160-270)
Aperçu rapide pour Neurofibromin 1 anticorps (AA 160-270) (ABIN7600195)
Antigène
Voir toutes Neurofibromin 1 (NF1) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 160-270
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Fonction
- Anti-Neurofibromin/NF1 Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Anti-Neurofibromin/NF1 Antibody (ABIN7600195). Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human Neurofibromin/NF1 recombinant protein (Position: R160-Q270).
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Isotype
- IgG
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Indications d'application
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Western blot, 0.25-0.5 μg/mL, Human
Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human
Immunocytochemistry/Immunofluorescence, 2 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
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- Neurofibromin 1 (NF1)
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Autre désignation
- NF1
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Sujet
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Synonyms: Neurofibromin, Neurofibromatosis-related protein NF-1, Neurofibromin truncated, NF1
Tissue Specificity: Detected in brain, peripheral nerve, lung, colon and muscle.
Background: Neurofibromin 1 (NF1) is a gene in humans that is located on chromosome 17. This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene.
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Poids moléculaire
- 319 kDa
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ID gène
- 4763
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UniProt
- P21359
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Pathways
- cAMP Metabolic Process, Regulation of long-term Neuronal Synaptic Plasticity
Antigène
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